Ma Siming, Yim Sun Hee, Lee Sang-Goo, Kim Eun Bae, Lee Sang-Rae, Chang Kyu-Tae, Buffenstein Rochelle, Lewis Kaitlyn N, Park Thomas J, Miller Richard A, Clish Clary B, Gladyshev Vadim N
Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA; Broad Institute, Cambridge, MA 02142, USA.
Cell Metab. 2015 Aug 4;22(2):332-43. doi: 10.1016/j.cmet.2015.07.005.
Biological diversity among mammals is remarkable. Mammalian body weights range seven orders of magnitude and lifespans differ more than 100-fold among species. While genetic, dietary, and pharmacological interventions can be used to modulate these traits in model organisms, it is unknown how they are determined by natural selection. By profiling metabolites in brain, heart, kidney, and liver tissues of 26 mammalian species representing ten taxonomical orders, we report metabolite patterns characteristic of organs, lineages, and species longevity. Our data suggest different rates of metabolite divergence across organs and reveal patterns representing organ-specific functions and lineage-specific physiologies. We identified metabolites that correlated with species lifespan, some of which were previously implicated in longevity control. We also compared the results with metabolite changes in five long-lived mouse models and observed some similar patterns. Overall, this study describes adjustments of the mammalian metabolome according to lifespan, phylogeny, and organ and lineage specialization.
哺乳动物之间的生物多样性十分显著。哺乳动物的体重范围跨越七个数量级,不同物种的寿命差异超过100倍。虽然可以通过基因、饮食和药物干预来调节模式生物的这些特征,但尚不清楚它们是如何由自然选择决定的。通过对代表十个分类目的26种哺乳动物的脑、心脏、肾脏和肝脏组织中的代谢物进行分析,我们报告了器官、谱系和物种寿命所特有的代谢物模式。我们的数据表明,不同器官的代谢物分化速率不同,并揭示了代表器官特定功能和谱系特定生理学的模式。我们鉴定出了与物种寿命相关的代谢物,其中一些代谢物以前曾被认为与寿命控制有关。我们还将结果与五个长寿小鼠模型中的代谢物变化进行了比较,并观察到了一些相似的模式。总体而言,这项研究描述了哺乳动物代谢组根据寿命、系统发育以及器官和谱系特化所做出的调整。